Drug Patent Number | Company | Drug Patent Title | Drug Patent Expiry | Activity Alert |
---|---|---|---|---|
These drug patents focus on the other aspects of the active substance like dosage, mode of administration (oral, tablet, capsules, liquids etc). | ||||
US6159498 | BDSI | Bioerodable film for delivery of pharmaceutical compounds of mucosal surfaces |
Oct, 2016
(7 years ago) | |
US7579019 | BDSI | Pharmaceutical carrier device suitable for delivery of pharmaceutical compounds to mucosal surfaces |
Jan, 2020
(4 years ago) | |
US9655843 | BDSI | Transmucosal delivery devices with enhanced uptake |
Jul, 2027
(3 years from now) | |
US8147866 | BDSI | Transmucosal delivery devices with enhanced uptake |
Jul, 2027
(3 years from now) | |
US8703177 | BDSI | Abuse-resistant mucoadhesive devices for delivery of buprenorphine |
Aug, 2032
(8 years from now) | |
US9522188 | BDSI | Abuse resistant transmucosal drug delivery device |
Apr, 2035
(11 years from now) |
Bunavail is owned by Bdsi.
Bunavail contains Buprenorphine Hydrochloride; Naloxone Hydrochloride.
Bunavail has a total of 6 drug patents out of which 2 drug patents have expired.
Expired drug patents of Bunavail are:
Bunavail was authorised for market use on 06 June, 2014.
Bunavail is available in film;buccal dosage forms.
Bunavail can be used as treatment of opioid dependence, maintenance treatment of opioid dependence.
The generics of Bunavail are possible to be released after 24 April, 2035.
Drug Exclusivity | Drug Exclusivity Expiration |
---|---|
New Product(NP) | Jun 06, 2017 |
Drugs and Companies using BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE ingredient
Market Authorisation Date: 06 June, 2014
Treatment: Maintenance treatment of opioid dependence; Treatment of opioid dependence
Dosage: FILM;BUCCAL